Showing 1 - 3 results of 3 for search 'Arthaporn Khongkraparn', query time: 0.05s Refine Results
  1. 1
    A Novel Homozygous PKP2 Variant in Severe Neonatal Non-compaction and Concomitant Ventricular Septal Defect: A Case Report

    A Novel Homozygous PKP2 Variant in Severe Neonatal Non-compaction and Concomitant Ventricular Septal Defect: A Case Report by Poomiporn Katanyuwong, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  2. 2
    A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficiency

    A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficie... by Pongpak Pongphitcha, Nongnuch Sirachainan, Arthaporn Khongkraparn, Thipwimol Tim-Aroon, Duantida Songdej, Duangrurdee Wattanasirichaigoon

    Published 2022
    Connect to this object online.
    Book
    Save to List
    Saved in:
  3. 3
    Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand

    Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand by Lukana Ngiwsara, Duangrurdee Wattanasirichaigoon, Thipwimol Tim-Aroon, Kitiwan Rojnueangnit, Saisuda Noojaroen, Arthaporn Khongkraparn, Phannee Sawangareetrakul, James R. Ketudat-Cairns, Ratana Charoenwattanasatien, Voraratt Champattanachai, Chulaluck Kuptanon, Suthipong Pangkanon, Jisnuson Svasti

    Published 2019
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: